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Purification of Sulfated Fucoglucuronomannan Lyase from Bacterial Strain of Fucobacter marina and Study of Appropriate Conditions for Its Enzyme Digestion

机译:滨海分枝杆菌细菌菌株中硫酸化葡糖醛糖醛酸甘露聚糖酶的纯化及酶消化的适宜条件研究

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摘要

A marine bacterial strain, Fucobacter marina, produced extracellular sulfated fucoglucuronomannan (SFGM) lyase when cultivated in the presence of crude SFGM obtained from fucoidan of Kjellmaniella crassifolia (brown algae) by cetyl pyridinium chloride fractionation. For the SFGM lyase assay, SFGM fraction separated from K. crassifolia fucoidan by anion exchange column chromatography was used as the substrate. The extracellular SFGM lyase was purified to homogeneity on an electrophoresis gel with 4240-fold purity at 13.8% yield. The enzyme proved to be a monomer, since gel filtration and sodium dodecyl sulfate polyacrylamide gel electrophoresis gave the same relative molecular mass of 67,000. The enzyme specifically digested SFGM but did not digest any other uronic-acid-containing polysaccharides tested. The optimum conditions for the enzyme reaction were around pH 7.5, 43 ℃, and 0.4 M NaCl concentration. The enzyme was strongly inhibited by CuCl_2 and ZnCl_2, and also by some sulfhydryl reagents.
机译:当在通过氯化十六烷基吡啶鎓盐分得自克耶尔曼氏菌藻(褐藻)的岩藻依聚糖而得的粗SFGM存在下培养时,海洋细菌菌株滨海Fucobacter marina产生了细胞外硫酸化的葡糖醛酸甘露聚糖(SFGM)裂解酶。对于SFGM裂解酶测定,将通过阴离子交换柱色谱法从红景天藻中分离出的SFGM级分用作底物。将细胞外SFGM裂解酶在电泳凝胶上纯化至均质,纯度为4240倍,产率为13.8%。该酶被证明是单体,因为凝胶过滤和十二烷基硫酸钠聚丙烯酰胺凝胶电泳得到的相对分子质量为67,000。该酶特异性消化SFGM,但不消化测试的任何其他含糖醛酸的多糖。酶反应的最佳条件为pH 7.5、43℃和0.4 M NaCl浓度。该酶被CuCl_2和ZnCl_2以及某些巯基试剂强烈抑制。

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